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N-Acetyltryptamine

From Wikipedia, the free encyclopedia
N-Acetyltryptamine
Names
IUPAC name
N-[2-(1H-indol-3-yl)ethyl]acetamide[1]
Other names
Acetotryptamide
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
  • InChI=1S/C12H14N2O/c1-9(15)13-7-6-10-8-14-12-5-3-2-4-11(10)12/h2-5,8,14H,6-7H2,1H3,(H,13,15)
    Key: NVUGEQAEQJTCIX-UHFFFAOYSA-N
  • CC(=O)NCCC1=CNC2=CC=CC=C21
Properties
C12H14N2O
Molar mass202.257 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

N-Acetyltryptamine (NAcT) is anorganic compound with themolecular formulaC12H14N2O. It is apartial agonist for themelatonin receptors.[2][3]N-Acetyltryptamine is produced byStreptomyces djakartensis and otherStreptomyces andFusarium species.[4][5]

See also

[edit]

References

[edit]
  1. ^"N-Acetyltryptamine".pubchem.ncbi.nlm.nih.gov.
  2. ^O'Brien, Paul (2 December 2012).Pineal and Retinal Relationships. Elsevier. p. 159.ISBN 978-0-323-14985-3.
  3. ^Current Trends in Comparative Endocrinology: Proceedings of the Ninth International Symposium on Comparative Endocrinology, Hong Kong, 7-11 December 1981. Kent State University Press.ISBN 978-962-209-116-0.
  4. ^Zhang, Wenjuan; Wei, Shaopeng; Zhang, Jiwen; Wu, Wenjun (1 March 2013)."Antibacterial Activity Composition of the Fermentation Broth of Streptomyces djakartensis NW35".Molecules.18 (3):2763–2768.doi:10.3390/molecules18032763.PMC 6270429.
  5. ^Paley, Elena L. (8 October 2020).Protein Biosynthesis Interference in Disease. Academic Press. p. 94.ISBN 978-0-12-823486-0.

Further reading

[edit]
  • Houlihan, William J. (15 September 2009).Indoles, Volume 25, Part 2. John Wiley & Sons. p. 25.ISBN 978-0-470-18841-5.
MT1Tooltip Melatonin receptor 1
MT2Tooltip Melatonin receptor 2
Unsorted
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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